Department of Surgery, Clinica Chirurgica, University of Cagliari, Ospedale San Giovanni di Dio, Via Ospedale 46, 09124, Cagliari, Italy.
World J Gastroenterol. 2010 Feb 7;16(5):648-51. doi: 10.3748/wjg.v16.i5.648.
This case report describes a woman with spontaneous rectal perforation from decidualized endometriosis in pregnancy. A 37-year-old woman was admitted to our hospital at 30 wk of pregnancy with symptoms suggestive of pyelonephritis, which persisted until 33 wk of gestation when delivery of a premature male baby was performed through a cesarean section. On postoperative day 2, an abdominal computed tomography showed free air in the peritoneal cavity and a pelvic abscess. Explorative celiotomy revealed a diffuse severe fecaloid peritonitis that originated from a 3-cm wide rectal perforation. A Hartmann operation was then performed. Histopathological findings were consistent with decidualization of the rectal wall. Only 20 cases of intestinal perforation due to endometriosis have been reported in the literature. This report is believed to be the first case of spontaneous rectal perforation from endometriosis in pregnancy, and it shows the potential occurrence of serious and unexpected complications of the disease.
本病例报告描述了一例妊娠期间蜕膜化子宫内膜异位症导致自发性直肠穿孔的患者。一名 37 岁女性在妊娠 30 周时因疑似肾盂肾炎入院,症状持续至妊娠 33 周时,通过剖宫产娩出一名早产男婴。术后第 2 天,腹部 CT 显示腹腔内有游离气体,盆腔脓肿。剖腹探查发现弥漫性严重粪性腹膜炎,起源于 3cm 宽的直肠穿孔。随后进行了 Hartmann 手术。组织病理学检查结果与直肠壁的蜕膜化一致。文献中仅报道了 20 例因子宫内膜异位症导致的肠穿孔。本报告被认为是首例妊娠期间自发性直肠穿孔的病例,它显示了这种疾病可能发生严重和意外的并发症。